N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

Base Information

Chemical Name:N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide
CAS No.:219519-40-1
Molecular Formula:C₂₅H₂₆N₄O₃
Molecular Weight:430.506
Hs Code.:

Synonyms:N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

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Chemical Property of N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

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Technology Process of N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

There total 6 articles about N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 42.0%

: 219519-39-8
N-(3-cyanophenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

: 219519-40-1
2-(4-t-butylbenzoylamino)-N-[3-(amino(hydroxyimino)methyl)phenyl]benzamide

Guidance literature:

Reference yield:

: 2237-30-1
m-cyanoaniline

: 219519-40-1
N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / pyridine / CH₂Cl₂ / 20 °C

2: 97 percent / H₂ / Pd/C / ethyl acetate

3: 92 percent / pyridine / CH₂Cl₂

4: 42 percent / NH₂OH*HCl; iPr₂NEt / ethanol / Heating

With pyridine; hydroxylamine hydrochloride; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate; 1: Acylation / 2: Reduction / 3: Acylation / 4: Addition;
DOI:10.1021/jm9903287

Reference yield:

: 610-14-0
2-nitrobenzyl chloride

: 219519-40-1
N-(3-(amino(hydroxyimino)methyl)phenyl)-2-(4-tert-butylbenzoyl)amino-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / pyridine / CH₂Cl₂ / 20 °C

2: 97 percent / H₂ / Pd/C / ethyl acetate

3: 92 percent / pyridine / CH₂Cl₂

4: 42 percent / NH₂OH*HCl; iPr₂NEt / ethanol / Heating

With pyridine; hydroxylamine hydrochloride; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate; 1: Acylation / 2: Reduction / 3: Acylation / 4: Addition;
DOI:10.1021/jm9903287